Bromide

Bromide

SCHEMBL490385

Br.CC1(c2c(-c3ccc(O)cc3)[nH]c3nccnc23)CC1

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3A P49840 19/20 0.59
GSK3B P49841 19/20 0.59
CDK1 P06493 18/20 0.59
CCNB2 O95067 17/20 0.59
CCNB1 P14635 17/20 0.59
CCNB3 Q8WWL7 17/20 0.59
CDK5 Q00535 13/20 0.59
CDK5R1 Q15078 12/20 0.59
MAPK8 P45983 3/20 0.51
CDK2 P24941 3/20 0.51
CCNE1 P24864 2/20 0.51
CCNE2 O96020 1/20 0.51
INSR P06213 1/20 0.51
CFTR P13569 1/20 0.51
CCNA2 P20248 1/20 0.51
MAPK3 P27361 1/20 0.51
MAPK1 P28482 1/20 0.51
MAPK9 P45984 1/20 0.51
MAPK10 P53779 1/20 0.51
CCNA1 P78396 1/20 0.51

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL490088 0.83 CCNB2 (0.63) GSK3AGSK3BCDK1CCNB2CCNB1
SCHEMBL490985 0.79 CDK1 (0.57) GSK3AGSK3BCDK1CCNB2CCNB1
SCHEMBL491139 0.77 CCNB2 (0.59) GSK3AGSK3BCDK1CCNB2CCNB1
Bromide SCHEMBL490592 0.77 GSK3A (0.97) GSK3AGSK3BCDK1CCNB2CCNB1
SCHEMBL16705135 0.71 GSK3A (0.74) GSK3AGSK3BCDK1CCNB2CCNB1
Bromide SCHEMBL490395 0.71 GSK3A (0.97) GSK3AGSK3BCDK1CCNB2CCNB1
Aloisine A SCHEMBL80147 0.68 GSK3A (1.00) GSK3AGSK3BCDK1CCNB2CCNB1
SCHEMBL13950079 0.68 GSK3A (0.60) GSK3AGSK3BCDK1CCNB2CCNB1
SCHEMBL7253117 0.64 GSK3A (0.69) GSK3AGSK3BCDK1CCNB2CCNB1
SCHEMBL1779469 0.64 GSK3A (0.69) GSK3AGSK3BCDK1CCNB2CCNB1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8106050-B2 6-[1-(4-Chlorophenyl)-1-cyclopropyl][5H]pyrrolo[2,3-b]pyrazine; cyclin-dependent kinases and glycogen synthase kinase-3 inhibitor; antiproliferative, anticarcinogenic agent; neurodegenerative disorders; controlling the cell cycle apoptosis, neuronal functions, transcription and exocytosis CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) 2012-01-31 US disclosed
US-20080161312-A1 Derivatives of Pyrrolo-Pyrazines Having a Kinase Inhibitory Activity and Their Biological Applications CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) 2008-07-03 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080161312-A1 Derivatives of Pyrrolo-Pyrazines Having a Kinase Inhibitory Activity and Their Biological Applications CDK2, PLK2, CDK5 GSK3A 656/4885GSK3B 599/4885CDK1 39/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.